← Back to catalogue

Fora

FDA UDI

Class II (US FDA UDI)

by Fora Care Inc.

Identity

Trade Name
FORA FDA UDI
Generic Name
Glucose IVD, kit, electrometry FDA UDI
Device Name
Blood Glucose Test Strips FDA UDI
Model / Reference
D40 Pro FDA UDI
Description
Blood Glucose Test Strips FDA UDI

Identifiers

Primary DI / UDI-DI
00816042012853 FDA UDI
510(k) Number
K101926 FDA UDI
FDA Product Code
CGA FDA UDI
GMDN Term
Glucose IVD, kit, electrometry FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1345 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Glucose IVD, kit, electrometry

Fora by Fora Care Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Glucose IVD, kit, electrometry.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Fora Care Inc.

Sources (1)

  • FDA UDI 43e6f9a7-e746-421b-9862-450e437b4ab2 34 fields · synced May 30, 2026